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Gene Symbol |
NR4A1 |
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Aliases |
GFRP1, HMR, N10, NAK-1, NGFIB, NP10, NUR77, TR3 |
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Entrez Gene ID |
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Gene Name |
Nuclear receptor subfamily 4 group A member 1 |
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Chromosomal Location |
12q13.13 |
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HGNC ID |
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Summary |
This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. Expression is induced by phytohemagglutinin in human lymphocytes and by serum stimulation of arrested fibroblasts. The encoded protein acts as a nuclear transcription factor. Translocation of the protein from the nucleus to mitochondria induces apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
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e!Ensembl
Gene |
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Transcript |
ENST00000548977, ENST00000546842, ENST00000553200, ENST00000545748, ENST00000550082, ENST00000550763, ENST00000394824, ENST00000548232, ENST00000562373, ENST00000550582, ENST00000394825, ENST00000360284, ENST00000243050 |
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Protein |
ENSP00000456633, ENSP00000457070, ENSP00000456776, ENSP00000440864, ENSP00000449539, ENSP00000449858, ENSP00000378301, ENSP00000449587, ENSP00000455399, ENSP00000455767, ENSP00000378302, ENSP00000353427, ENSP00000243050
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Gene Ontology (GO)
GO ID |
Ontology |
Function |
Evidence |
Reference |
GO:0001938 |
Biological process |
Positive regulation of endothelial cell proliferation |
IMP |
18059339 |
GO:0002042 |
Biological process |
Cell migration involved in sprouting angiogenesis |
IDA |
18059339 |
GO:0007165 |
Biological process |
Signal transduction |
TAS |
2626032 |
GO:0035767 |
Biological process |
Endothelial cell chemotaxis |
IMP |
18059339 |
GO:0035924 |
Biological process |
Cellular response to vascular endothelial growth factor stimulus |
IMP |
18059339 |
GO:0044344 |
Biological process |
Cellular response to fibroblast growth factor stimulus |
IMP |
18059339 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IDA |
22427340 |
GO:0071376 |
Biological process |
Cellular response to corticotropin-releasing hormone stimulus |
IBA |
21873635 |
GO:0005634 |
Cellular component |
Nucleus |
IBA |
21873635 |
GO:0005667 |
Cellular component |
Transcription factor complex |
IBA |
21873635 |
GO:0000977 |
Molecular function |
RNA polymerase II regulatory region sequence-specific DNA binding |
IBA |
21873635 |
GO:0000978 |
Molecular function |
RNA polymerase II proximal promoter sequence-specific DNA binding |
IBA |
21873635 |
GO:0000981 |
Molecular function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
ISM |
19274049 |
GO:0000981 |
Molecular function |
DNA-binding transcription factor activity, RNA polymerase II-specific |
NAS |
19274049 |
GO:0005515 |
Molecular function |
Protein binding |
IPI |
17139261, 18305892, 18835031, 18985028, 19095693, 20195357, 21988832, 22761572, 24139859, 25416956 |
GO:0035259 |
Molecular function |
Glucocorticoid receptor binding |
IBA |
21873635 |
GO:0043565 |
Molecular function |
Sequence-specific DNA binding |
IBA |
21873635 |
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Protein Information |
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Protein Name |
Nuclear receptor subfamily 4 group A member 1, ST-59, TR3 orphan receptor, early response protein NAK1, growth factor-inducible nuclear protein N10, hormone receptor, nerve growth factor IB nuclear receptor variant 1, nuclear hormone receptor NUR/77, orphan nuclear receptor HMR, orphan nuclear receptor TR3, steroid receptor TR3, testicular receptor 3 |
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Function |
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UniProt |
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PDB |
2QW4, 3V3E, 3V3Q, 4JGV, 4KZI, 4KZJ, 4KZM, 4RE8, 4REE, 4REF, 4RZE, 4RZF, 4RZG, 4WHF, 4WHG |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000440864 |
P22736 |
P22736 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Blood Disorders |
Myelodysplastic Syndrome |
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Cardiovascular Diseases |
Ventricular Fibrillation |
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Atherosclerosis |
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Cardiomyopathy |
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Digestive System Diseases |
Inflammatory Bowel Diseases |
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Liver Diseases |
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Endocrine System Diseases |
PCOS |
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Hyperandrogenism |
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Diabetes Mellitus |
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Adrenal Cortex Diseases |
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Neoplasms |
Colonic Neoplasms |
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Lymphoma |
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Ovarian Cancer |
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Breast Cancer |
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Pancreatic Neoplasm |
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Gastric Cancer |
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Rhabdomyoma |
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Adrenal Cancer |
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Myeloid Leukemia |
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Leydig Cell Tumor |
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Liver Cancer |
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Squamous Cell Carcinoma |
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Nervous System Diseases |
Seizures |
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Epilepsy |
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Dyskinesia |
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Nutritional and Metabolic Diseases |
Hypercholesterolemia |
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Obesity |
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Hyperinsulinism |
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Reproductive disorders |
Endometriosis |
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Respiratory Tract Diseases |
Pulmonary Fibrosis |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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PCOS, Lipid and Steroid metabolism |
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Rotterdam Criteria |
Direct
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79 PCOs patients and 93 controls |
The results of qPCR showed that the expression of related genes were in accordance with the RNA-seq analysis results. |
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